GB587333A - Improvements in or relating to the production of resinous compositions - Google Patents

Improvements in or relating to the production of resinous compositions

Info

Publication number
GB587333A
GB587333A GB450/45A GB45045A GB587333A GB 587333 A GB587333 A GB 587333A GB 450/45 A GB450/45 A GB 450/45A GB 45045 A GB45045 A GB 45045A GB 587333 A GB587333 A GB 587333A
Authority
GB
United Kingdom
Prior art keywords
acids
glycol
ketals
acetals
oils
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired
Application number
GB450/45A
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Imperial Chemical Industries Ltd
Original Assignee
Imperial Chemical Industries Ltd
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Imperial Chemical Industries Ltd filed Critical Imperial Chemical Industries Ltd
Publication of GB587333A publication Critical patent/GB587333A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08FMACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
    • C08F8/00Chemical modification by after-treatment

Landscapes

  • Chemical & Material Sciences (AREA)
  • General Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Organic Chemistry (AREA)
  • Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)
  • Lubricants (AREA)
  • Paints Or Removers (AREA)

Abstract

Polyvinyl ketals or acetals, or mixtures of both, are heated together with a polyhydric alcohol ester, which has been completely esterified with a non-hydroxylated mono-basic carboxylic acid containing at least 6 carbon atoms, at a temperature of at least 100 DEG C. to give a mixture which is homogeneous at ordinary temperatures. The amount of acetal or ketal is usually between 20 per cent and 80 per cent of the total weight of the mixture. The acid constituents of the esters include saturated or unsaturated monobasic aliphatic, cycloaliphatic, aromatic and carboxylic acids. Those preferred are the long chain aliphatic acids containing from 12 to 18 carbon atoms, particularly such acids derived from the non-hydroxylated natural oils. Suitable acids are caproic, caprylic, capric, lauric, myristic, palmitic, stearic, melissic, beta-furyl acrylic, sorbic, undecylenic, oleic, elaidic, linoleic, linolenic, nonadecanoic, behenic, cyclohexane carboxylic, benzoic, abietic and naphthenic, and the mixed acids derived from unmodified oils such as linseed, chinawood, soya bean, sunflower, perilla, oiticica, olive, palm, seal and lard oils. Preferred esters are triglycerides such as these natural oils. The polyhydric alcohol constituents include ethylene glycol, glycerol, diethylene glycol, polyethylene glycol, pentaerythritol, mannitol, sorbitol, octamethylene glycol and decamethylene glycol. Specified acetals are those derived from formaldehyde, acetaldehyde, butyraldehyde, propionaldehyde, heptaldehyde, citral, benzaldehyde, salicylaldehyde, p - nitrobenzaldehyde, cinnamaldehyde, p-chlorobenzaldehyde, anisaldehyde and furfural; and ketals those derived from acetone, 2,2-diethoxy butane, mesityl oxide, phorone, cyclohexanone, acetophenone, p-nitro- and p-chloro-acetophenone, benzophenone, benzalacetophenone, pulezone and methyl-2-thienyl ketone. Mixed acetals or ketals may be used. Examples illustrate the use of the product in coating compositions using toluene or ethyl alcohol and xylene as solvents and containing cobalt, manganese, lead or iron naphthenate as a drier. Other materials such as pigments, synthetic or natural resins, plasticisers, fillers, waxes, oxidation inhibitors, catalysts and solvents, of which many examples are specified, may be added.
GB450/45A 1943-10-15 1945-01-05 Improvements in or relating to the production of resinous compositions Expired GB587333A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US587333XA 1943-10-15 1943-10-15

Publications (1)

Publication Number Publication Date
GB587333A true GB587333A (en) 1947-04-22

Family

ID=22018593

Family Applications (1)

Application Number Title Priority Date Filing Date
GB450/45A Expired GB587333A (en) 1943-10-15 1945-01-05 Improvements in or relating to the production of resinous compositions

Country Status (1)

Country Link
GB (1) GB587333A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN113993910A (en) * 2019-03-18 2022-01-28 芬欧汇川集团 Method for preparing thermoplastic polyvinyl alcohol derivative by molten state reaction and product thereof

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN113993910A (en) * 2019-03-18 2022-01-28 芬欧汇川集团 Method for preparing thermoplastic polyvinyl alcohol derivative by molten state reaction and product thereof

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